Evidence map›Paper›PMID 31511580›Full record

ArticleScientific reports2019

Ixodes scapularis salivary gland microRNAs are differentially expressed during Powassan virus transmission.

Meghan E Hermance, Steven G Widen, Thomas G Wood, Saravanan Thangamani

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  11. Analysis ofbioRxiv : the preprint server for biology · 2024
    Article
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  14. Analysis ofFrontiers in cellular and infection microbiology · 2024
    Article
  15. Article
  16. Article
  17. Identification of microRNAs in the Lyme Disease VectorInternational journal of molecular sciences · 2022
    Article
  18. What do we know about the microbiome ofFrontiers in cellular and infection microbiology · 2022
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Meghan E HermanceSUNY Center for Environmental Health and Medicine, SUNY Upstate Medical University, Syracuse, NY, United States.
Steven G WidenDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, United States.
Thomas G WoodDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, United States.
Saravanan ThangamaniSUNY Center for Environmental Health and Medicine, SUNY Upstate Medical University, Syracuse, NY, United States. ThangamS@upstate.edu.ORCID http://orcid.org/0000-0002-4269-5993
SUNY Upstate Medical University · USThe University of Texas Medical Branch at Galveston · US

Funding

TICK DETERMINANTS OF POWASSAN VIRUS TRANSMISSIONR01AI127771 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI THANGAMANI, SARAVANAN · 2017 to 2021
$2.0M
NIAID NIH HHS R01 AI127771
6 · The paper itself

Abstract

Successful tick feeding is facilitated by an assortment of pharmacologically-active factors in tick saliva that create an immunologically privileged micro-environment in the host's skin. Through a process known as saliva-assisted transmission, bioactive tick salivary factors modulate the host environment, promoting transmission and establishment of a tick-borne pathogen. This phenomenon was previously demonstrated for Powassan virus (POWV), a North American tick-borne flavivirus that is the causative agent of a severe neuroinvasive disease in humans. Here, we sought to characterize the Ixodes scapularis salivary gland microRNAs (miRNAs) expressed during the earliest period of POWV transmission to a mammalian host. POWV-infected and uninfected I. scapularis females were fed on naïve mice for 1, 3, and 6 hours, and Illumina next generation sequencing was used to characterize the salivary gland miRNA expression profiles of POWV-infected versus uninfected ticks. 379 salivary miRNAs were detected, of which 338 are reported here as putative novel I. scapularis miRNAs. 35 salivary gland miRNAs were significantly up-regulated and 17 miRNAs were significantly down-regulated in response to POWV infection. To investigate the potential role of salivary gland miRNAs in POWV replication in-vitro, we transfected miRNA inhibitors into VeroE6 cells to profile temporal POWV replication in mammalian cells. Together, the small RNA sequencing data and the in vitro miRNA inhibition assay suggest that the differentially expressed tick salivary miRNAs could act in regulating POWV replication in host tissues.

Indexed as

AnimalsEncephalitis, Tick-BorneEncephalitis Viruses, Tick-BorneFemaleHost-Pathogen InteractionsIxodesMiceMice, Inbred C57BLMicroRNAsSalivary GlandsMicroRNAs

Identifiers

PMID31511580
PMCPMC6739385
OpenAlexW2972341024

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.